Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H17F3N2O4 |
| Molecular Weight | 406.3552 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=CC2=C1C(O)=C(C(=O)N(C)C3=CC=C(C=C3)C(F)(F)F)C(=O)N2C
InChI
InChIKey=ONDYALNGTUAJDX-UHFFFAOYSA-N
InChI=1S/C20H17F3N2O4/c1-24(12-9-7-11(8-10-12)20(21,22)23)18(27)16-17(26)15-13(25(2)19(16)28)5-4-6-14(15)29-3/h4-10,26H,1-3H3
| Molecular Formula | C20H17F3N2O4 |
| Molecular Weight | 406.3552 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P06702 Gene ID: 6280.0 Gene Symbol: S100A9 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/27298414 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
0.26 μM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/19755981/ |
0.5 mg 1 times / day steady-state, oral dose: 0.5 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
TASQUINIMOD plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
4.8 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/19755981/ |
0.5 mg 1 times / day steady-state, oral dose: 0.5 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
TASQUINIMOD plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
40 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/19755981/ |
0.5 mg 1 times / day steady-state, oral dose: 0.5 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
TASQUINIMOD plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Tasquinimod Is an Allosteric Modulator of HDAC4 survival signaling within the compromised cancer microenvironment. | 2013-02-15 |
|
| The long and winding road for the development of tasquinimod as an oral second-generation quinoline-3-carboxamide antiangiogenic drug for the treatment of prostate cancer. | 2010-10 |
|
| Angiogenesis inhibitors in the treatment of prostate cancer. | 2010-08-02 |
|
| Tasquinimod (ABR-215050), a quinoline-3-carboxamide anti-angiogenic agent, modulates the expression of thrombospondin-1 in human prostate tumors. | 2010-05-17 |
|
| Open-label, clinical phase I studies of tasquinimod in patients with castration-resistant prostate cancer. | 2009-10-20 |
|
| The quinoline-3-carboxamide anti-angiogenic agent, tasquinimod, enhances the anti-prostate cancer efficacy of androgen ablation and taxotere without effecting serum PSA directly in human xenografts. | 2007-05-15 |
|
| Identification of ABR-215050 as lead second generation quinoline-3-carboxamide anti-angiogenic agent for the treatment of prostate cancer. | 2006-12-01 |
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01234311
Tasquinimod is given orally at a dose of 1 mg once daily.
Route of Administration:
Oral
LNCaP prostate tumor cells were cultured with 50 uM of tasquinimod for 24 h to test its effect on gene expression. At 10 uM tasquinimod the TSP1 mRNA expression was elevated at 6 h and peaked after 72 h. Moreover, after 72 h exposure the TSP1 mRNA levels was already elevated at a dose of 1 uM tasquinimod.
| Substance Class |
Chemical
Created
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| Record UNII |
756U07KN1R
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Validated (UNII)
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Official Name | English | ||
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NCI_THESAURUS |
C1742
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FDA ORPHAN DRUG |
561916
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NCI_THESAURUS |
C129820
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FDA ORPHAN DRUG |
877022
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C74080
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756U07KN1R
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8538
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TASQUINIMOD
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DB05861
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SUB88412
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C516109
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CHEMBL2107784
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m10480
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PRIMARY | Merck Index |
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ACTIVE MOIETY |
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